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Package 'MEDIPS' - Bioconductor

Package 'MEDIPS' - Bioconductor

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4 MEDIPS.addCNV<br />

chr_lengths: Object of class "numeric" : the lengths of the chromosomes included within the<br />

MEDIPS/COUPLING SET<br />

seq_pattern: Object of class "character" : the sequence pattern (e.g. CG)<br />

genome_CF: Object of class "numeric" : the coupling factor at the genomic bins<br />

number_pattern: Object of class "numeric" : the total number of sequence pattern<br />

Methods<br />

genome_name signature(object = "COUPLINGset"): extracts the reference genome of the<br />

COUPLING SET<br />

window_size signature(object = "COUPLINGset"): extracts the window size from the window_size<br />

slot COUPLING SET<br />

chr_names signature(object = "COUPLINGset"): extracts the names of the chromosomes<br />

included within the COUPLING SET<br />

chr_lengths signature(object = "COUPLINGset"): extracts the length of the chromosomes<br />

included within the COUPLING SET<br />

seq_pattern signature(object = "COUPLINGset"): extracts the sequence pattern (e.g. CpG)<br />

genome_CF signature(object = "COUPLINGset"): extracts the coupling factor at the genomic<br />

bins<br />

number_pattern signature(object = "COUPLINGset"): extracts the total number of sequence<br />

pattern<br />

show signature(object = "COUPLINGset"): prints a summary of the COUPLING SET object<br />

content<br />

Author(s)<br />

Lukas Chavez, Matthias Lienhard, Joern Dietrich<br />

Examples<br />

showClass("COUPLINGset")<br />

MEDIPS.addCNV<br />

Function to run a copy number variation analysis.<br />

Description<br />

Function calculates a CNV analysis based on two INPUT SETs by employing the DNAcopy package.<br />

The results are attached to a provided result table.<br />

Usage<br />

MEDIPS.addCNV(ISet1, ISet2, results, cnv.Frame=1000)

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